Clinical Research Directory

Inclusion Criteria: * Clinical Dementia Rating 0.5 - 2 * Be a person with or caregiver to a person with a diagnosis of early Alzheimer's Disease, mild dementia, and/or mild cognitive impairment (MCI) and chronic pain defined as non-cancer pain lasting \>3 months that occurs most days and limits life or work activities OR Be a caregiver to a person with a diagnosis of early Alzheimer's Disease, mild dementia, and/or mild cognitive impairment (MCI) and chronic pain defined as non-cancer pain lasting \>3 months that occurs most days and limits life or work activities * Able to provide informed consent * Willing to wear an EEG headset and heart rate monitoring devices * Willing to answer survey questions about topics related to the study * Willing to be audio / video recorded * Willing to undergo QST, blood draw, heart rate data collection and cognitive testing Exclusion Criteria: * Clinical Dementia Rating \<0.5 or \> 2 * Unable to provide informed consent * Endorsing suicidal ideation (SI), self-injurious behavior, or homicidal ideation (HI) above the threshold defined in the "Risk Reduction and Safety Plan" * Participating in another clinical trial studying AD and/or Dementia * Starting a new prescription medication in the last 4 weeks * Taking central nervous system acting medications that may interfere with study measurements as determined at PI discretion